Validation of eDNA as a viable method of detection for dangerous cubozoan jellyfish

Abstract Stings from certain species of cubozoan jellyfish are dangerous to humans and their seasonal presence in tropical marine waters poses a significant risk to coastal communities. The detection of cubozoans is difficult due to high spatial and temporal variation in their occurrence and abundan...

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Main Authors: Brett Bolte, Julie Goldsbury, Roger Huerlimann, Dean Jerry, Michael Kingsford
Format: Article
Language:English
Published: Wiley 2021-07-01
Series:Environmental DNA
Subjects:
Online Access:https://doi.org/10.1002/edn3.181
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author Brett Bolte
Julie Goldsbury
Roger Huerlimann
Dean Jerry
Michael Kingsford
author_facet Brett Bolte
Julie Goldsbury
Roger Huerlimann
Dean Jerry
Michael Kingsford
author_sort Brett Bolte
collection DOAJ
description Abstract Stings from certain species of cubozoan jellyfish are dangerous to humans and their seasonal presence in tropical marine waters poses a significant risk to coastal communities. The detection of cubozoans is difficult due to high spatial and temporal variation in their occurrence and abundance. Environmental DNA (eDNA) has the potential to detect rare species and therefore offers potential to detect cubozoans, not only pelagic medusae, but presence of cryptic polyp life stages. The objective of this study was to validate the use of eDNA as a viable detection method for four cubozoan species (Chironex fleckeri, Copula sivickisi, Carybdea xaymacana, and Carukia barnesi). Species‐specific primers were developed for each of these four cubozoans and an eDNA approach validated utilizing both laboratory and field trials. Laboratory DNA degradation experiments demonstrated that C. sivickisi DNA degraded quickly but could still be detected in sea water for up to 9 days post‐jellyfish removal. Positive detection was found for C. fleckeri, C. xaymacana, and C. sivickisi medusae in the waters surrounding Magnetic Island, Queensland, in the Austral spring/summer (September‐January). Based on visual surveys, there was a poor relationship between concentration of eDNA and abundance of jellyfish. Positive eDNA amplification was also found from water sampled near the substratum when C. sivickisi medusae were out of season and absent. This suggests the eDNA analysis was likely detecting C. sivickisi polyps located within the substratum. Consequently, eDNA is an effective tool to detect both the medusae and likely polyps of cubozoans. This approach provides the means to reduce the risk of envenomation to swimmers and enhance our knowledge of cubozoan ecology.
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spelling doaj.art-ec0e66f48cb64e0489dc5fc0c73458e92022-12-21T22:08:00ZengWileyEnvironmental DNA2637-49432021-07-013476977910.1002/edn3.181Validation of eDNA as a viable method of detection for dangerous cubozoan jellyfishBrett Bolte0Julie Goldsbury1Roger Huerlimann2Dean Jerry3Michael Kingsford4Marine Biology and Aquaculture College of Science and Engineering James Cook University Townsville QLD AustraliaMarine Biology and Aquaculture College of Science and Engineering James Cook University Townsville QLD AustraliaMarine Biology and Aquaculture College of Science and Engineering James Cook University Townsville QLD AustraliaMarine Biology and Aquaculture College of Science and Engineering James Cook University Townsville QLD AustraliaMarine Biology and Aquaculture College of Science and Engineering James Cook University Townsville QLD AustraliaAbstract Stings from certain species of cubozoan jellyfish are dangerous to humans and their seasonal presence in tropical marine waters poses a significant risk to coastal communities. The detection of cubozoans is difficult due to high spatial and temporal variation in their occurrence and abundance. Environmental DNA (eDNA) has the potential to detect rare species and therefore offers potential to detect cubozoans, not only pelagic medusae, but presence of cryptic polyp life stages. The objective of this study was to validate the use of eDNA as a viable detection method for four cubozoan species (Chironex fleckeri, Copula sivickisi, Carybdea xaymacana, and Carukia barnesi). Species‐specific primers were developed for each of these four cubozoans and an eDNA approach validated utilizing both laboratory and field trials. Laboratory DNA degradation experiments demonstrated that C. sivickisi DNA degraded quickly but could still be detected in sea water for up to 9 days post‐jellyfish removal. Positive detection was found for C. fleckeri, C. xaymacana, and C. sivickisi medusae in the waters surrounding Magnetic Island, Queensland, in the Austral spring/summer (September‐January). Based on visual surveys, there was a poor relationship between concentration of eDNA and abundance of jellyfish. Positive eDNA amplification was also found from water sampled near the substratum when C. sivickisi medusae were out of season and absent. This suggests the eDNA analysis was likely detecting C. sivickisi polyps located within the substratum. Consequently, eDNA is an effective tool to detect both the medusae and likely polyps of cubozoans. This approach provides the means to reduce the risk of envenomation to swimmers and enhance our knowledge of cubozoan ecology.https://doi.org/10.1002/edn3.181cubozoanenvironmental DNAIrukandjijellyfishPCR
spellingShingle Brett Bolte
Julie Goldsbury
Roger Huerlimann
Dean Jerry
Michael Kingsford
Validation of eDNA as a viable method of detection for dangerous cubozoan jellyfish
Environmental DNA
cubozoan
environmental DNA
Irukandji
jellyfish
PCR
title Validation of eDNA as a viable method of detection for dangerous cubozoan jellyfish
title_full Validation of eDNA as a viable method of detection for dangerous cubozoan jellyfish
title_fullStr Validation of eDNA as a viable method of detection for dangerous cubozoan jellyfish
title_full_unstemmed Validation of eDNA as a viable method of detection for dangerous cubozoan jellyfish
title_short Validation of eDNA as a viable method of detection for dangerous cubozoan jellyfish
title_sort validation of edna as a viable method of detection for dangerous cubozoan jellyfish
topic cubozoan
environmental DNA
Irukandji
jellyfish
PCR
url https://doi.org/10.1002/edn3.181
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